Molecular Dynamics Modeling of the Interaction of Cationic Fluorescent Lipid Peroxidation-Sensitive Probes with the Mitochondrial Membrane
- Authors: Nesterenko A.M.1,2, Kholina E.G.3, Lyamzaev K.G.1, Mulkidjanian A.Y.1,3,4, Chernyak B.V.1
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Affiliations:
- Belozersky Institute of Physico-Chemical Biology, Moscow State University
- Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry Russian Academy of Sciences
- Moscow State University
- Faculty of Physics, University of Osnabrück
- Issue: Vol 486, No 1 (2019)
- Pages: 220-223
- Section: Biochemistry, Biophysics, and Molecular Biology
- URL: https://journal-vniispk.ru/1607-6729/article/view/213035
- DOI: https://doi.org/10.1134/S1607672919030153
- ID: 213035
Cite item
Abstract
Cardiolipin (CL) plays a central role in lipid peroxidation (LPO) of the mitochondrial inner membrane due to higher content of unsaturated fatty acids in CL in comparison with the other phospholipids. CL oxidation plays an important role in the regulation of various intracellular signaling pathways and its excessive oxidation contributes to the development of various pathologies and, possibly, participates in the aging process. Mitochondria-targeted antioxidants containing triphenylphosphonium (TPP+) effectively protect CL from oxidation. It is assumed that fluorescent probes on the basis of the C11-BODIPY fluorophore sensitive to LPO and containing TPP+ can selectively register CL oxidation. To test this possibility, we carried out a molecular dynamic simulation of such probes in a model mitochondrial membrane. It is shown that the probes are located in the membrane at the same depth as the unsaturated bonds in CL molecules sensitive to oxidation. Increasing the length of the linker that binds the fluorophore and TPP+ residue ha little effect on the position of the probe in the membrane. This indicates the possibility of modifying the linker to increase the selectivity of the probes to CL.
About the authors
A. M. Nesterenko
Belozersky Institute of Physico-Chemical Biology,Moscow State University; Shemyakin and Ovchinnikov Institute
of Bioorganic Chemistry Russian Academy of Sciences
Email: bchernyak@yahoo.com
Russian Federation, Moscow; Moscow
E. G. Kholina
Moscow State University
Email: bchernyak@yahoo.com
Russian Federation, Moscow
K. G. Lyamzaev
Belozersky Institute of Physico-Chemical Biology,Moscow State University
Email: bchernyak@yahoo.com
Russian Federation, Moscow
A. Ya. Mulkidjanian
Belozersky Institute of Physico-Chemical Biology,Moscow State University; Moscow State University; Faculty of Physics, University of Osnabrück
Email: bchernyak@yahoo.com
Russian Federation, Moscow; Moscow;
Osnabrück
B. V. Chernyak
Belozersky Institute of Physico-Chemical Biology,Moscow State University
Author for correspondence.
Email: bchernyak@yahoo.com
Russian Federation, Moscow
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